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卵巢中肾样腺癌:病例研究

Mesonephric-like adenocarcinoma of the ovary: a case study.

作者信息

Assila Saad, Khmou Mouna, Mahdi Youssef, El Khannoussi Basma

机构信息

Department of Pathology of the National Institute of Oncology, Ibn Sina University Hospital Center, Allal Al Fassi Avenue, Rabat 10100, Morocco.

Department of Pathology, Faculty of Medicine and Pharmacy, Mohammed V University, Mohamed Belarbi Alaoui Avenue, Rabat 10000, Morocco.

出版信息

J Surg Case Rep. 2025 Jan 26;2025(1):rjaf025. doi: 10.1093/jscr/rjaf025. eCollection 2025 Jan.

Abstract

Mesonephric-like adenocarcinoma (MLA) is a rare and newly recognized subtype of ovarian and endometrial carcinomas, introduced in the 2020 World Health Organization Classification. This tumor likely originates from Müllerian-derived tissues and often mimics more common ovarian cancers, leading to frequent misdiagnosis. This case study details a 36-year-old woman who presented with urinary symptoms following a hysterectomy. Imaging revealed a significant left ovarian mass, initially misdiagnosed as carcinosarcoma. Pathological evaluation ultimately confirmed MLA, characterized by diverse architectural patterns and specific immunohistochemical markers. The patient underwent chemotherapy due to the locally advanced disease. This case highlights the diagnostic challenges of MLA and emphasizes the need for awareness among clinicians to prevent misdiagnosis. Given its aggressive nature and tendency to early recurrence, further research is essential for establishing standardized diagnostic criteria and treatment protocols for this rare malignancy.

摘要

中肾样腺癌(MLA)是一种罕见的、新认识的卵巢癌和子宫内膜癌亚型,于2020年被纳入世界卫生组织分类。这种肿瘤可能起源于苗勒管来源的组织,常与更常见的卵巢癌相似,导致频繁误诊。本病例研究详细介绍了一名36岁女性,她在子宫切除术后出现泌尿系统症状。影像学检查发现左侧卵巢有一个较大肿块,最初被误诊为癌肉瘤。病理评估最终确诊为MLA,其特征为多种结构模式和特定的免疫组化标志物。由于疾病局部进展,患者接受了化疗。本病例突出了MLA的诊断挑战,并强调临床医生需要提高认识以防止误诊。鉴于其侵袭性和早期复发倾向,进一步研究对于建立这种罕见恶性肿瘤的标准化诊断标准和治疗方案至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ad/11767864/03fb0ef480f4/rjaf025f1.jpg

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